HGVS | Genome Assembly |
---|---|
NC_000006.12:g.52236960C>T , CM000668.2:g.52236960C>T | GRCh38 |
NC_000006.11:g.52101758C>T , CM000668.1:g.52101758C>T | GRCh37 |
NC_000006.10:g.52209717C>T | NCBI36 |
NG_031869.1:g.12541G>A , LRG_356:g.12541G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000699946.1:c.463G>A | ENSP00000514702.1:p.Val155Ile | |
ENST00000336123.5:c.463G>A MANE Select | ENSP00000337432.4:p.Val155Ile | |
ENST00000336123.4:c.463G>A | ENSP00000337432.4:p.Val155Ile | |
ENST00000478427.1:n.647G>A | ||
NM_052872.3:c.463G>A , LRG_356t1:c.463G>A | NP_443104.1:p.Val155Ile | |
XM_011514276.1:c.463G>A | XP_011512578.1:p.Val155Ile | |
NM_052872.4:c.463G>A MANE Select | NP_443104.1:p.Val155Ile |